Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264319생성일: 2026년 10월 25일
Hydroxyamine hydrochloride → N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide
https://huagongshe.com/reaction/264319
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | Ethyl 2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetate | HCID 10834775 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide | HCID 10738924 | — |
반응 단계
Ethyl 2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetate (1.22 g, 3.05 mmol) is dissolved in methanol (15 mL). To this solution is added hydroxylamine hydrochloride (0.43 g, 6.11 mmol), followed by the addition of sodium methoxide, freshly prepared from sodium (0.35 g, 15.3 mmol) dissolved in methanol (5 mL). The reaction is stirred for 36 hours at room temperature. The reaction is worked up by partitioning between dilute hydrochloric acid (pH=~3) and ethyl acetate. The aqueous phase is extracted well with ethyl acetate, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is crystallized from hexnae/ethyl acetate and collected by filtration to give N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide, m.p. 108°-110° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05646167 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-0b55bed1ad31402aa6efa71dcdffe34c |
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| 출처 메모 | uspto-grants-1997_07 |
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